Molecular Imaging Program, Center for Cancer Research, National Cancer Institute, NIH , Bethesda, Maryland 20892, United States.
Mol Pharm. 2017 Dec 4;14(12):4628-4635. doi: 10.1021/acs.molpharmaceut.7b00731. Epub 2017 Nov 22.
Near-infrared photoimmunotherapy (NIR-PIT) is a newly developed cancer treatment that induces highly selective immunogenic cell death. It is based on an antibody-photoabsorber conjugate (APC) that is activated by NIR light. The purpose of this study was to investigate the effects of NIR-PIT as measured by luciferase-luciferin photon-counting and fluorescence imaging. Six days after subcutaneous injection of A431-luc-GFP cells tumors formed in a xenograft mouse model. The EGFR-targeting antibody, panitumumab, was conjugated to the photoabsorber, IRDye-700DX (pan-IR700), and was intravenously administered to tumor-bearing mice. Serial luciferase-luciferin photon-counting images and both green fluorescent protein (GFP) and IR700 fluorescence images were obtained from the same mice before and after NIR-PIT treatment (0, 10, 20, 30 min (early phase), and 24, 48 h (late phase) after NIR light exposure). Optical signal intensities were compared for each modality. IR700 fluorescence and luciferase-luciferin photon-counting images showed decreased intensities in both the early and late phases after NIR-PIT (p < 0.01). On the other hand, GFP fluorescence images showed decreased intensities only in the late phase (p < 0.01). In the early phase, GFP fluorescence images showed smaller intensity reductions compared to IR700 fluorescence and luciferase-luciferin photon-counting (p < 0.01), while in the late phase, IR700 fluorescence showed smaller intensity reductions than luciferase-luciferin photon-counting and GFP fluorescence (p < 0.05), due to redistribution of pan-IR700 within the tumor bed. In conclusion, luciferase-luciferin photon-counting imaging is suitable to evaluate early phase NIR-PIT effects, while both luciferase-luciferin photon-counting and GFP reflected later phase effects.
近红外光免疫治疗(NIR-PIT)是一种新开发的癌症治疗方法,可诱导高度选择性免疫原性细胞死亡。它基于抗体-光吸收剂偶联物(APC),该偶联物可被近红外光激活。本研究旨在通过荧光素酶-荧光素光子计数和荧光成像来研究 NIR-PIT 的效果。在异种移植小鼠模型中,A431-luc-GFP 细胞皮下注射 6 天后形成肿瘤。将针对 EGFR 的抗体,panitumumab 与光吸收剂 IRDye-700DX(pan-IR700)偶联,并静脉注射到荷瘤小鼠体内。在 NIR-PIT 治疗前后(NIR 光暴露后 0、10、20、30 分钟(早期)和 24、48 小时(晚期)),从同一只小鼠获得连续的荧光素酶-荧光素光子计数图像以及 GFP 和 IR700 荧光图像。比较每种模态的光信号强度。NIR-PIT 后早期和晚期,IR700 荧光和荧光素酶-荧光素光子计数图像的强度均降低(p <0.01)。另一方面,GFP 荧光图像仅在晚期显示出强度降低(p <0.01)。在早期,与 IR700 荧光和荧光素酶-荧光素光子计数相比,GFP 荧光图像的强度降低较小(p <0.01),而在晚期,IR700 荧光的强度降低小于荧光素酶-荧光素光子计数和 GFP 荧光(p <0.05),这是由于 pan-IR700 在肿瘤床内重新分布所致。总之,荧光素酶-荧光素光子计数成像适合评估 NIR-PIT 的早期效果,而荧光素酶-荧光素光子计数和 GFP 均反映了后期效果。